prajmaline and Coronary-Disease

prajmaline has been researched along with Coronary-Disease* in 4 studies

Trials

1 trial(s) available for prajmaline and Coronary-Disease

ArticleYear
Effects of oral prajmaline bitartrate on exercise test responses in patients with coronary artery disease.
    European journal of clinical pharmacology, 1985, Volume: 28, Issue:4

    The safety, tolerability and haemodynamic effects of oral prajmaline bitartrate were assessed in a double-blind, randomized, placebo-controlled, crossover trial in 21 patients with stable angina pectoris and coronary artery disease. No serious side-effects occurred. Prajmaline bitartrate produced no statistically significant changes in resting heart rate or systolic blood pressure or in work capacity on the treadmill, or in heart rate or systolic blood pressure at maximum exercise compared to placebo values. No new arrhythmias or conduction abnormalities were produced in any patient. We conclude that oral prajmaline bitartrate is well tolerated and can be given safely to patients with coronary artery disease without producing deleterious haemodynamic effects or changes in exercise capacity.

    Topics: Administration, Oral; Adult; Aged; Ajmaline; Coronary Disease; Exercise Test; Hemodynamics; Humans; Male; Middle Aged; Prajmaline

1985

Other Studies

3 other study(ies) available for prajmaline and Coronary-Disease

ArticleYear
[Anti-arrhythmic effectiveness of neogilurhythmal in extrasystolic arrhythmia].
    Kardiologiia, 1992, Volume: 32, Issue:6

    The paper provides the results of differential neogilurythmal therapy in 20 patients with high-grade atrial and ventricular premature contractions in the presence of coronary heart disease. The detection of cardiac arrhythmias and evaluation of the antiarrhythmic efficacy of neogilurythmal were performed by Holter monitoring and transesophageal electrophysiological study. After the baseline studies, the antiarrhythmic efficacy of the drug was evaluated during an acute drug test and then during a 8-day course of the therapy. In the acute drug test, the dose of neogilurythmal was 50% of the daily dosage. The studies indicated that neogilurythmal in a dose of 80 mg/day was beneficial in affecting both the atrial and ventricular extrasystolic arrhythmia. The agent failed to alter heart rate, sinus nodal function and atrioventricular conduction. Thus, neogilurythmal is low toxic and produces no adverse effects when given in the definite dosage range.

    Topics: Adult; Cardiac Complexes, Premature; Child; Coronary Disease; Electrocardiography; Female; Humans; Male; Middle Aged; Prajmaline

1992
Acute haemodynamic effects of ajmaline and prajmaline in patients with coronary heart disease.
    European journal of clinical pharmacology, 1984, Volume: 26, Issue:2

    Thirty patients undergoing cardiac catheterisation for coronary artery disease received parenteral ajmaline (15 patients) or prajmaline (15 patients). There were no statistically significant induced changes in left ventricular systolic or end diastolic pressures, indirect left atrial pressure, pulmonary artery mean pressure, cardiac output or left ventricular ejection fraction compared to control values. Intravenous prajmaline bitartrate in 15 patients with angina did not significantly alter work capacity, maximum exercise heart rate or systolic blood pressure compared to control values. Five patients developed transient minor conduction defects ( 2LBBB , 1 RBBB, 2 prolonged PR interval): all five were also receiving long-term treatment with beta blockers and nifedipine.

    Topics: Adult; Ajmaline; Angina Pectoris; Blood Pressure; Cardiac Catheterization; Cardiac Output; Coronary Disease; Female; Heart Ventricles; Hemodynamics; Humans; Infusions, Parenteral; Male; Middle Aged; Physical Exertion; Prajmaline

1984
[Atenolol versus prajmalium bitartrate. Double-blind study on the treatment of ventricular extrasystoles in coronary heart disease].
    MMW, Munchener medizinische Wochenschrift, 1982, Aug-27, Volume: 124, Issue:34

    Topics: Ajmaline; Atenolol; Cardiac Complexes, Premature; Coronary Disease; Double-Blind Method; Female; Heart Ventricles; Humans; Male; Middle Aged; Prajmaline; Propanolamines

1982